184 related articles for article (PubMed ID: 11027508)
1. Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency.
Horvath R; Lochmüller H; Stucka R; Yao J; Shoubridge EA; Kim SH; Gerbitz KD; Jaksch M
Biochem Biophys Res Commun; 2000 Sep; 276(2):530-3. PubMed ID: 11027508
[TBL] [Abstract][Full Text] [Related]
2. Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase.
Leary SC; Kaufman BA; Pellecchia G; Guercin GH; Mattman A; Jaksch M; Shoubridge EA
Hum Mol Genet; 2004 Sep; 13(17):1839-48. PubMed ID: 15229189
[TBL] [Abstract][Full Text] [Related]
3. Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.
Papadopoulou LC; Sue CM; Davidson MM; Tanji K; Nishino I; Sadlock JE; Krishna S; Walker W; Selby J; Glerum DM; Coster RV; Lyon G; Scalais E; Lebel R; Kaplan P; Shanske S; De Vivo DC; Bonilla E; Hirano M; DiMauro S; Schon EA
Nat Genet; 1999 Nov; 23(3):333-7. PubMed ID: 10545952
[TBL] [Abstract][Full Text] [Related]
4. The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasis.
Leary SC; Cobine PA; Kaufman BA; Guercin GH; Mattman A; Palaty J; Lockitch G; Winge DR; Rustin P; Horvath R; Shoubridge EA
Cell Metab; 2007 Jan; 5(1):9-20. PubMed ID: 17189203
[TBL] [Abstract][Full Text] [Related]
5. Cytochrome c oxidase deficiency.
Shoubridge EA
Am J Med Genet; 2001; 106(1):46-52. PubMed ID: 11579424
[TBL] [Abstract][Full Text] [Related]
6. Ortholog search of proteins involved in copper delivery to cytochrome C oxidase and functional analysis of paralogs and gene neighbors by genomic context.
Arnesano F; Banci L; Bertini I; Martinelli M
J Proteome Res; 2005; 4(1):63-70. PubMed ID: 15707358
[TBL] [Abstract][Full Text] [Related]
7. SCO1 and SCO2 act as high copy suppressors of a mitochondrial copper recruitment defect in Saccharomyces cerevisiae.
Glerum DM; Shtanko A; Tzagoloff A
J Biol Chem; 1996 Aug; 271(34):20531-5. PubMed ID: 8702795
[TBL] [Abstract][Full Text] [Related]
8. Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethality.
Tay SK; Shanske S; Kaplan P; DiMauro S
Arch Neurol; 2004 Jun; 61(6):950-2. PubMed ID: 15210538
[TBL] [Abstract][Full Text] [Related]
9. Molecular characterization of Saccharomyces cerevisiae Sco2p reveals a high degree of redundancy with Sco1p.
Lode A; Paret C; Rödel G
Yeast; 2002 Aug; 19(11):909-22. PubMed ID: 12125048
[TBL] [Abstract][Full Text] [Related]
10. Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.
Sue CM; Karadimas C; Checcarelli N; Tanji K; Papadopoulou LC; Pallotti F; Guo FL; Shanske S; Hirano M; De Vivo DC; Van Coster R; Kaplan P; Bonilla E; DiMauro S
Ann Neurol; 2000 May; 47(5):589-95. PubMed ID: 10805329
[TBL] [Abstract][Full Text] [Related]
11. Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency.
Tay SK; Nesti C; Mancuso M; Schon EA; Shanske S; Bonilla E; Davidson MM; Dimauro S
Arch Neurol; 2004 Dec; 61(12):1935-7. PubMed ID: 15596615
[TBL] [Abstract][Full Text] [Related]
12. SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome.
Zhu Z; Yao J; Johns T; Fu K; De Bie I; Macmillan C; Cuthbert AP; Newbold RF; Wang J; Chevrette M; Brown GK; Brown RM; Shoubridge EA
Nat Genet; 1998 Dec; 20(4):337-43. PubMed ID: 9843204
[TBL] [Abstract][Full Text] [Related]
13. Human cytochrome oxidase deficiency.
Robinson BH
Pediatr Res; 2000 Nov; 48(5):581-5. PubMed ID: 11044474
[TBL] [Abstract][Full Text] [Related]
14. The P(174)L mutation in the human hSCO1 gene affects the assembly of cytochrome c oxidase.
Paret C; Lode A; Krause-Buchholz U; Rödel G
Biochem Biophys Res Commun; 2000 Dec; 279(2):341-7. PubMed ID: 11118289
[TBL] [Abstract][Full Text] [Related]
15. Human recombinant mutated forms of the mitochondrial COX assembly Sco2 protein differ from wild-type in physical state and copper binding capacity.
Foltopoulou PF; Zachariadis GA; Politou AS; Tsiftsoglou AS; Papadopoulou LC
Mol Genet Metab; 2004 Mar; 81(3):225-36. PubMed ID: 14972329
[TBL] [Abstract][Full Text] [Related]
16. Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene.
Vesela K; Hulkova H; Hansikova H; Zeman J; Elleder M
APMIS; 2008 Jan; 116(1):41-9. PubMed ID: 18254779
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiency.
Péquignot MO; Dey R; Zeviani M; Tiranti V; Godinot C; Poyau A; Sue C; Di Mauro S; Abitbol M; Marsac C
Hum Mutat; 2001 May; 17(5):374-81. PubMed ID: 11317352
[TBL] [Abstract][Full Text] [Related]
18. Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1.
Leary SC; Sasarman F; Nishimura T; Shoubridge EA
Hum Mol Genet; 2009 Jun; 18(12):2230-40. PubMed ID: 19336478
[TBL] [Abstract][Full Text] [Related]
19. Specific copper transfer from the Cox17 metallochaperone to both Sco1 and Cox11 in the assembly of yeast cytochrome C oxidase.
Horng YC; Cobine PA; Maxfield AB; Carr HS; Winge DR
J Biol Chem; 2004 Aug; 279(34):35334-40. PubMed ID: 15199057
[TBL] [Abstract][Full Text] [Related]
20. Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency.
Darin N; Moslemi AR; Lebon S; Rustin P; Holme E; Oldfors A; Tulinius M
Neuropediatrics; 2003 Dec; 34(6):311-7. PubMed ID: 14681757
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
